Evidence map›Paper›PMID 40909519›Full record

ArticlebioRxiv : the preprint server for biology2025

Teneurin-3 and latrophilin-2 are required for somatotopic map formation and somatosensory topognosis.

Kevin T Sangster, Xinying Zhang, Daniel Del Toro, Christina Sarantopoulos, Ashley M Moses, Shreya Mahasenan, Daniel T Pederick, Sophie Perreault, Catherine Fallet-Bianco, R Brian Roome and 3 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Kevin T SangsterInstitut de Recherches Cliniques de Montréal (IRCM); Montréal, QC, Canada.
Xinying ZhangInstitut de Recherches Cliniques de Montréal (IRCM); Montréal, QC, Canada.
Daniel Del ToroDepartment of Biomedical Sciences, Faculty of Medicine and Health Sciences, Institute of Neurosciences, IDIBAPS, CIBERNED; University of Barcelona, Barcelona, Spain.
Christina SarantopoulosInstitut de Recherches Cliniques de Montréal (IRCM); Montréal, QC, Canada.
Ashley M MosesDepartment of Biology, Howard Hughes Medical Institute, Stanford University; Stanford, CA, USA.
Shreya MahasenanInstitut de Recherches Cliniques de Montréal (IRCM); Montréal, QC, Canada.
Daniel T PederickDepartment of Biology, Howard Hughes Medical Institute, Stanford University; Stanford, CA, USA.
Sophie PerreaultAzrieli Research Center at CHU Sainte-Justine; Montréal, QC, Canada.
Catherine Fallet-BiancoDepartment of Pathology, CHU Sainte-Justine; Montréal, QC, Canada.
R Brian RoomeSpinal Circuits and Plasticity Unit, National Institute of Neurological Disorders and Stroke; Bethesda, MD, USA.
Elena SeiradakeDepartment of Biochemistry, Oxford University; Oxford, UK.
Liqun LuoDepartment of Biology, Howard Hughes Medical Institute, Stanford University; Stanford, CA, USA.
Artur KaniaInstitut de Recherches Cliniques de Montréal (IRCM); Montréal, QC, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Somatotopy is a recurring organisational feature of the somatosensory system where adjacent neurons and their connections represent adjacent regions of the body. The molecular mechanisms governing the formation of such "body maps" remain largely unknown. Here we demonstrate that the cell surface proteins teneurin-3 and latrophilin-2 are expressed in opposing gradients in multiple somatotopic maps in the mouse, including within the dorsal horn of the spinal cord. Genetic manipulation of these proteins in spinal dorsal horn or sensory neurons distorts the somatotopy of neuronal connections and impairs accurate localisation of a noxious stimulus on the surface of the body. Our work provides the foundation for a molecular model of somatotopic map formation and insights into their function in the localisation of somatosensory stimuli or topognosis.

Identifiers

PMID40909519
PMCPMC12407721

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.